structure of 5-carbamoyl-1-methylpyrrole-3-sulfonyl chloride

5-carbamoyl-1-methylpyrrole-3-sulfonyl chloride

CAS No.: 1000931-98-5
M. Wt: 222.65
M. Fa: C6H7ClN2O3S
InChI Key: -

Names and Identifiers of 1000931-98-5

CAS Number

1000931-98-5

IUPAC Name

5-aminocarbonyl-1-methyl-pyrrole-3-sulfonyl chloride

Canonical SMILES

CN1C=C(C=C1C(=O)N)S(=O)(=O)Cl

Physical and chemical properties of 1000931-98-5

Acidity coefficient

14.55±0.50(Predicted)

Boiling Point

404.9±30.0 °C(Predicted)

Density

1.65±0.1 g/cm3(Predicted)

Molecular Formula

C6H7ClN2O3S

Molecular Weight

222.65

Safety Information of 1000931-98-5

Pictograms

Signal Word

 Danger

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000931-98-5

5-Carbamoyl-1-methyl-1H-pyrrole-3-sulfonyl chloride has potential applications in:

  • Medicinal Chemistry: As a building block for synthesizing biologically active compounds.
  • Agricultural Chemistry: In developing pesticides or herbicides due to its reactive functional groups.
  • Material Science: As a precursor for synthesizing polymers or materials with specific properties.

Its unique structure allows it to act as an intermediate in various chemical syntheses, making it valuable in industrial applications.

Interaction Studies of 1000931-98-5

Interaction studies involving 5-carbamoyl-1-methyl-1H-pyrrole-3-sulfonyl chloride are essential for understanding its reactivity and potential biological effects. Preliminary studies may focus on its interactions with nucleophiles such as amines or alcohols, assessing reaction kinetics and mechanisms. Furthermore, studying its biological interactions could reveal insights into its pharmacological potential and toxicity profiles.

Biological Activity of 1000931-98-5

While specific biological activity data for 5-carbamoyl-1-methyl-1H-pyrrole-3-sulfonyl chloride is limited, compounds containing pyrrole and sulfonyl functionalities often exhibit significant pharmacological properties. Pyrrole derivatives have been studied for their potential anti-inflammatory, antimicrobial, and anticancer activities. The presence of the sulfonamide moiety may also enhance the compound's bioactivity by improving solubility and interaction with biological targets.